RECRUITING

Using AI and Peer Coaching to Address Racial Disparities Among People Who Use Opioids

Study Overview

This clinical trial focuses on testing the efficacy of different digital interventions to promote re-engagement in cancer-related long-term follow-up care for adolescent and young adult (AYA) survivors of childhood cancer.

Description

Black and Latinx people who use opioids are disproportionately impacted by opioid overdose deaths. The proposed study assesses the efficacy of an open source, multimodal artificial intelligence-driven texting tool combined with peer recovery coach-supported text contact that delivers social services, stigma reduction, health habitus, and patient navigation content addressing social determinants of health to enhance receipt of buprenorphine in primary care among emergency department-enrolled Black / Latinx people who use opioids.

Official Title

Leveraging Social Determinants Via Artificial Intelligence and Peer Coaching to Address Racial Disparities in Primary Care Among People Who Use Opioids

Quick Facts

Study Start:2024-01-07
Study Completion:2026-08-31
Study Type:Not specified
Phase:Not Applicable
Enrollment:Not specified
Status:RECRUITING

Study ID

NCT06569667

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Ages Eligible for Study:18 Years to 99 Years
Sexes Eligible for Study:ALL
Accepts Healthy Volunteers:No
Standard Ages:ADULT, OLDER_ADULT
Inclusion CriteriaExclusion Criteria
  1. 1. ≥18 years of age;
  2. 2. fluent in English and/or Spanish;
  3. 3. self-reported non-prescription opioid use \<30 days prior to consent;
  4. 4. provision of informed consent;
  5. 5. planned stay in NYC ≥12 month;
  6. 6. self-identified Black and/or Latinx race/ethnicity;
  7. 7. positive urine toxicology for opioids per EMR records;
  8. 8. diagnosis of OUD per the Diagnostic and Statistical Manual of Mental Disorders-5
  9. 9. self-reported interest in initiating buprenorphine in primary care
  10. 10. must have a mobile phone data plan.
  1. 1. inability to comprehend text content written at a 3rd grade reading level;
  2. 2. physical or visual disability preventing mobile phone use;
  3. 3. self-reported receipt of medications for OUD in past 30 days.

Contacts and Locations

Study Contact

Babak Toighi, MSc, MD
CONTACT
4102947477
babak.tofighi@nki.rfmh.org

Study Locations (Sites)

NYC Health + Hospitals
Bronx, New York, 10451
United States

Collaborators and Investigators

Sponsor: Friends Research Institute, Inc.

Study Record Dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Registration Dates

Study Start Date2024-01-07
Study Completion Date2026-08-31

Study Record Updates

Study Start Date2024-01-07
Study Completion Date2026-08-31

Terms related to this study

Keywords Provided by Researchers

  • Opioid Use Disorder
  • Peer Recovery Coach
  • AI-driven text tool
  • mobile health (mHealth)

Additional Relevant MeSH Terms

  • Opioid Use Disorder